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University Medical Center Groningen
Department of Genetics -
L1CAM Mutation Database
Introduction
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Mutations
Protein domains
References
Mutation Details
DNA change
Protein change
Exon/intron
Type
Reported classification
Bateman
SIFT
PolyPhen
Conserved
Protein domain
Remarks
LOVD ID
c.1340_1353del14
p.Leu447ArgfsX40
Exon 11
Deletion; frameshift
Disease-causing
n.a.
n.a.
n.a.
n.a.
Ig 5
Patients
Family
# Affected relatives
Clinical features
Remarks
Reference
1
2
(Dys)agenesis corpus callosum, Hydrocephalus
Two brothers: >7 yrs and > 5,5 yrs
Graf et al. (2000)
References
Year
Author
Title
Journal
Volume
Pages
Weblink
2000
Graf et al.
Diffusion-weighted magnetic resonance imaging in boys with neural cell adhesion molecule L1 mutations and congenital hydrocephalus
Ann. Neurol.
47
113-117
10632110